Mori T - Search Results

1

Gains, losses, and amplifications of genomic materials in primary gastric cancers analyzed by comparative genomic hybridization.

Sakakura C, Mori T, Sakabe T, Ariyama Y, Shinomiya T, Date K, Hagiwara A, Yamaguchi T, Takahashi T, Nakamura Y, Abe T, Inazawa J. Sakakura C, et al. Among authors: mori t. Genes Chromosomes Cancer. 1999 Apr;24(4):299-305. doi: 10.1002/(sici)1098-2264(199904)24:4<299::aid-gcc2>3.0.co;2-u. Genes Chromosomes Cancer. 1999. PMID: 10092127

2

Loss of material from chromosome arm 1p during malignant progression of meningioma revealed by fluorescent in situ hybridization.

Ishino S, Hashimoto N, Fushiki S, Date K, Mori T, Fujimoto M, Nakagawa Y, Ueda S, Abe T, Inazawa J. Ishino S, et al. Among authors: mori t. Cancer. 1998 Jul 15;83(2):360-6. Cancer. 1998. PMID: 9669820

3

Identification of a novel gene, MASL1, within an amplicon at 8p23.1 detected in malignant fibrous histiocytomas by comparative genomic hybridization.

Sakabe T, Shinomiya T, Mori T, Ariyama Y, Fukuda Y, Fujiwara T, Nakamura Y, Inazawa J. Sakabe T, et al. Among authors: mori t. Cancer Res. 1999 Feb 1;59(3):511-5. Cancer Res. 1999. PMID: 9973190

4

Comparative genomic hybridization of squamous cell carcinoma of the esophagus: the possible involvement of the DPI gene in the 13q34 amplicon.

Shinomiya T, Mori T, Ariyama Y, Sakabe T, Fukuda Y, Murakami Y, Nakamura Y, Inazawa J. Shinomiya T, et al. Among authors: mori t. Genes Chromosomes Cancer. 1999 Apr;24(4):337-44. Genes Chromosomes Cancer. 1999. PMID: 10092132

5

Chromosomal imbalances in adult T-cell leukemia revealed by comparative genomic hybridization: gains at 14q32 and 2p16-22 in cell lines.

Ariyama Y, Mori T, Shinomiya T, Sakabe T, Fukuda Y, Kanamaru A, Yamada Y, Isobe M, Seto M, Nakamura Y, Inazawa J. Ariyama Y, et al. Among authors: mori t. J Hum Genet. 1999;44(6):357-63. doi: 10.1007/s100380050178. J Hum Genet. 1999. PMID: 10570904

6

Identification of amplified DNA sequences on double minute chromosomes in a leukemic cell line KY821 by means of spectral karyotyping and comparative genomic hybridization.

Ariyama Y, Sakabe T, Shinomiya T, Mori T, Fukuda Y, Inazawa J. Ariyama Y, et al. Among authors: mori t. J Hum Genet. 1998;43(3):187-90. doi: 10.1007/s100380050067. J Hum Genet. 1998. PMID: 9747033

7

Frequent multiplication of the long arm of chromosome 8 in hepatocellular carcinoma.

Fujiwara Y, Monden M, Mori T, Nakamura Y, Emi M. Fujiwara Y, et al. Among authors: mori t. Cancer Res. 1993 Feb 15;53(4):857-60. Cancer Res. 1993. PMID: 8381331

8

Allelotype study of esophageal carcinoma.

Aoki T, Mori T, Du X, Nisihira T, Matsubara T, Nakamura Y. Aoki T, et al. Among authors: mori t. Genes Chromosomes Cancer. 1994 Jul;10(3):177-82. doi: 10.1002/gcc.2870100305. Genes Chromosomes Cancer. 1994. PMID: 7522040

9

Frequent loss of heterozygosity in the region including BRCA1 on chromosome 17q in squamous cell carcinomas of the esophagus.

Mori T, Aoki T, Matsubara T, Iida F, Du X, Nishihira T, Mori S, Nakamura Y. Mori T, et al. Among authors: mori s. Cancer Res. 1994 Apr 1;54(7):1638-40. Cancer Res. 1994. PMID: 7907942

10

Frequent somatic mutation of the MTS1/CDK4I (multiple tumor suppressor/cyclin-dependent kinase 4 inhibitor) gene in esophageal squamous cell carcinoma.

Mori T, Miura K, Aoki T, Nishihira T, Mori S, Nakamura Y. Mori T, et al. Among authors: mori s. Cancer Res. 1994 Jul 1;54(13):3396-7. Cancer Res. 1994. PMID: 8012957

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